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vero african green monkey kidney epithelial cells  (ATCC)


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    ATCC vero african green monkey kidney epithelial cells
    Vero African Green Monkey Kidney Epithelial Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 18165 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/african+green+monkey+kidney+epithelial+vero+cells/Vero/pm42886552-360-0-7
    Average 99 stars, based on 18165 article reviews
    vero african green monkey kidney epithelial cells - by Bioz Stars, 2026-11
    99/100 stars

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    other:

    Article Title: Venezuelan Equine Encephalitis Virus Antagonizes the cGAS-STING Pathway.
    Article Snippet: Human microglial cells (HMC3) (ATCC, CRL-3304, Manassas, VA, USA) were maintained in Eagle’s Minimum Essential Medium with L-glutamine (EMEM) (Quality Biological, 112-018-101, Gaithersburg, MD, USA) supplemented with 10% fetal bovine serum (FBS) (Avantor, 97068-085, Radnor, PA, USA) and 1% penicillin/streptomycin (Pen-Strep) (Quality Biological, 120-095-721, Gaithersburg, MD, USA).

    Article Title: Venezuelan Equine Encephalitis Virus Antagonizes the cGAS-STING Pathway
    Article Snippet: Human microglial cells (HMC3) (ATCC, CRL-3304, Manassas, VA, USA) were maintained in Eagle’s Minimum Essential Medium with L-glutamine (EMEM) (Quality Biological, 112-018-101, Gaithersburg, MD, USA) supplemented with 10% fetal bovine serum (FBS) (Avantor, 97068-085, Radnor, PA, USA) and 1% penicillin/streptomycin (Pen-Strep) (Quality Biological, 120-095-721, Gaithersburg, MD, USA).

    Modification:

    Article Title: Enhancing the virulence of G2a subtype PEDV by chimeric expression of G2c subtype S gene.
    Article Snippet: Among the various causes of pig diarrhea, porcine epidemic diarrhea (PED) remains a severe disease causing significant economic losses to the global swine industry.. Given the rapid variation of the PEDV spike (S) protein, it is crucial to investigate how S protein of different genotypes influence the pathogenicity and immunogenicity of PEDV.. Herein, chimeric PEDV strains were constructed by inserting the S gene of subtype G1b, G2b, or G2c into the corresponding position of the G2a subtype strain GX4/2021 using Red recombination.

    Article Title: Antiviral efficacy of silicon nitride against SARS-CoV-2 and MERS-CoV: implications for PPE innovation
    Article Snippet: .. African green monkey kidney epithelial (Vero) cells (ATCC, CCL-81) were maintained in Dulbecco’s Modified Eagle Medium (DMEM) (VWR, 10128-208) supplemented with 10% fetal bovine serum (FBS) (VWR, 97068-085), 1% L-glutamine (VWR, 45000-676), and 1% penicillin/streptomycin (VWR, 45000-652). .. Vero E6 cells (ATCC, CRL-1586) were maintained in Eagle’s Minimum Essential Medium with L-glutamine (EMEM) (VWR, 10128-608) supplemented with 10% FBS and 1% penicillin/streptomycin.

    Cell Culture:

    Article Title: Manipulating Zika virus RNA tertiary structure for developing tissue-specific attenuated vaccines
    Article Snippet: .. The baby hamster kidney fibroblast (BHK-21) cells (ATCC CCL10), African green monkey kidney epithelial (Vero) cells (ATCC CCL81) were cultured in DMEM (Thermo Fisher Scientific) containing 7% fetal bovine serum (FBS, Biowest). .. A549 cells (ATCC CRM-CCL-185) were cultured in DMEM containing 10% FBS.

    Article Title: Activation of the stress-activated protein kinase JNK in response to herpes simplex virus-1 infection coordinates transition of BRD4 from chromosome association to transcription elongation
    Article Snippet: .. The human cervical carcinoma HeLa cells (ATCC, CCL-2), HEK293T cells (ATCC, CRL-3216), and African green monkey kidney epithelial Vero cells (ATCC, CCL-81) were cultured in DMEM (high glucose) supplemented with 10% heat-inactivated fetal bovine serum (FBS), non-essential amino acids (Life Technologies) and sodium pyruvate at 37 °C in a humidified incubator with 5% CO 2 . .. The human cervical carcinoma HeLa cells (ATCC, CCL-2), HEK293T cells (ATCC, CRL-3216), and African green monkey kidney epithelial Vero cells (ATCC, CCL-81) were cultured in DMEM (high glucose) supplemented with 10% heat-inactivated fetal bovine serum (FBS), non-essential amino acids (Life Technologies) and sodium pyruvate at 37 °C in a humidified incubator with 5% CO 2 .

    Article Title: Ginsenoside Rb2 demonstrates potent antiviral activity against Zika virus infection
    Article Snippet: Aedes albopictus clone C6/36 cells (ATCC-CRL-1660) were cultured in Dulbecco's Modified Eagle's medium (DMEM). .. SK-N-SH (SK) cells (ATCC-HTB-11) and African green monkey kidney epithelial Vero cells (CCL-81, American Type Culture Collection) were cultured in Minimum Essential Medium (MEM). .. CCF-STTG1 (CCF) cells (ATCC-CRL-1718) were cultured in RPMI 1640.



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    ATCC african green monkey kidney epithelial cell line vero
    Optimization of cell-related conditions for the RSV mRNA potency assay. ( A ) Dose–response curves of RSV mRNA transfection in different cell lines (293T, <t>Vero,</t> HEp-2, HepG2, and A549). Cells were transfected with increasing amounts of RSV mRNA (0.0002–0.48 µg/well), and RSV prefusion F protein expression was measured by ELISA as OD 450 –OD 630 . The corresponding EC 50 and slope values are summarized in the inset table. ( B ) Effect of HepG2 cell seeding density on RSV prefusion F protein expression. HepG2 cells were seeded at 0.5 × 10 5 , 1.0 × 10 5 , or 2.0 × 10 5 cells/well and transfected with increasing amounts of RSV mRNA (0.0002–0.48 µg/well). Protein expression was measured by ELISA as OD 450 –OD 630 .
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    ATCC african green monkey kidney epithelial vero e6 cells
    (A-P) Caco-2 and RFe-ATC cells were infected for 72 h. Caco-2 cells were infected with SARS-CoV-2 (A-D) or BANAL-236 (I-L) at an MOI 0.001 and 0.01 respectively. RFe-ATC cells were infected with SARS-CoV-2 (E-H) and BANAL-236 ( M-P ) at MOI 0.02 and 0.2 respectively. Cells were then subjected to transmission electron microscopy analysis. DMV-like structures are pointed by white arrows. (Q-R) At 48 and 72 h post-infection supernatants from Caco-2 (Q) and RFe-ATC (R) cells were collected. Titration of clarified supernatants by TCID 50 assays was performed <t>on</t> <t>Vero-E6</t> cells infected for 5 days. Data are the means ± SEM of at least two independent experiments.
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    Optimization of cell-related conditions for the RSV mRNA potency assay. ( A ) Dose–response curves of RSV mRNA transfection in different cell lines (293T, Vero, HEp-2, HepG2, and A549). Cells were transfected with increasing amounts of RSV mRNA (0.0002–0.48 µg/well), and RSV prefusion F protein expression was measured by ELISA as OD 450 –OD 630 . The corresponding EC 50 and slope values are summarized in the inset table. ( B ) Effect of HepG2 cell seeding density on RSV prefusion F protein expression. HepG2 cells were seeded at 0.5 × 10 5 , 1.0 × 10 5 , or 2.0 × 10 5 cells/well and transfected with increasing amounts of RSV mRNA (0.0002–0.48 µg/well). Protein expression was measured by ELISA as OD 450 –OD 630 .

    Journal: Vaccines

    Article Title: Establishment and Validation of a Cell-Based Relative Potency Method for Respiratory Syncytial Virus mRNA Vaccine Drug Substance

    doi: 10.3390/vaccines14050401

    Figure Lengend Snippet: Optimization of cell-related conditions for the RSV mRNA potency assay. ( A ) Dose–response curves of RSV mRNA transfection in different cell lines (293T, Vero, HEp-2, HepG2, and A549). Cells were transfected with increasing amounts of RSV mRNA (0.0002–0.48 µg/well), and RSV prefusion F protein expression was measured by ELISA as OD 450 –OD 630 . The corresponding EC 50 and slope values are summarized in the inset table. ( B ) Effect of HepG2 cell seeding density on RSV prefusion F protein expression. HepG2 cells were seeded at 0.5 × 10 5 , 1.0 × 10 5 , or 2.0 × 10 5 cells/well and transfected with increasing amounts of RSV mRNA (0.0002–0.48 µg/well). Protein expression was measured by ELISA as OD 450 –OD 630 .

    Article Snippet: Cell lines used for mRNA transfection included the human liver carcinoma cell line HepG2 (American Type Culture Collection, ATCC, Manassas, VA, USA), human non-small cell lung carcinoma cell line A549 (ATCC), African green monkey kidney epithelial cell line Vero (ATCC), human epidermoid carcinoma type 2 cell line Hep-2 (ATCC), and human embryonic kidney cell line 293T (China Center for Type Culture Collection, CCTCC, Wuhan, China).

    Techniques: Potency Assay, Transfection, Expressing, Enzyme-linked Immunosorbent Assay

    (A-P) Caco-2 and RFe-ATC cells were infected for 72 h. Caco-2 cells were infected with SARS-CoV-2 (A-D) or BANAL-236 (I-L) at an MOI 0.001 and 0.01 respectively. RFe-ATC cells were infected with SARS-CoV-2 (E-H) and BANAL-236 ( M-P ) at MOI 0.02 and 0.2 respectively. Cells were then subjected to transmission electron microscopy analysis. DMV-like structures are pointed by white arrows. (Q-R) At 48 and 72 h post-infection supernatants from Caco-2 (Q) and RFe-ATC (R) cells were collected. Titration of clarified supernatants by TCID 50 assays was performed on Vero-E6 cells infected for 5 days. Data are the means ± SEM of at least two independent experiments.

    Journal: PLOS Pathogens

    Article Title: Entry, replication and innate immunity evasion of BANAL-236, a SARS-CoV-2-related bat virus, in Rhinolophus and human cells

    doi: 10.1371/journal.ppat.1013573

    Figure Lengend Snippet: (A-P) Caco-2 and RFe-ATC cells were infected for 72 h. Caco-2 cells were infected with SARS-CoV-2 (A-D) or BANAL-236 (I-L) at an MOI 0.001 and 0.01 respectively. RFe-ATC cells were infected with SARS-CoV-2 (E-H) and BANAL-236 ( M-P ) at MOI 0.02 and 0.2 respectively. Cells were then subjected to transmission electron microscopy analysis. DMV-like structures are pointed by white arrows. (Q-R) At 48 and 72 h post-infection supernatants from Caco-2 (Q) and RFe-ATC (R) cells were collected. Titration of clarified supernatants by TCID 50 assays was performed on Vero-E6 cells infected for 5 days. Data are the means ± SEM of at least two independent experiments.

    Article Snippet: Human colorectal adenocarcinoma Caco-2 cells (kind gift from Nathalie Sauvonnet, Institut Pasteur, Paris), African green monkey kidney epithelial Vero-E6 cells (ATCC CRL-1586), A549 lung cancer cells (ATCC CCL-185), and human embryonic kidney (HEK) 293T cells (ATCC CRL-3216), hereinafter referred to as 293T, were maintained in Dulbecco’s Modified Eagle Medium (DMEM) (Gibco) containing GlutaMAX I, sodium pyruvate (Invitrogen) supplemented with 10% heat-inactivated fetal bovine serum (FBS) (Dutscher) and 1% penicillin and streptomycin (10 000 IU/ml; Thermo Fisher Scientific).

    Techniques: Infection, Transmission Assay, Electron Microscopy, Titration